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      Synthesis of Thermo-Responsive Polymer via Radical (Co)polymerization of N, N-Dimethyl-α-(hydroxymethyl)acrylamide with N,N-Diethylacrylamide

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          Abstract

          α-Functionalized acrylamides have not been considered as an effective monomer design due to their poor polymerizability, although the analogues, α-functionalized acrylates, are attractive monomers of which polymers exhibit characteristic properties. In this article, we report the first example of radical polymerization of α-functionalized N, N-disubstituted acrylamide affording thermo-responsive hydrophilic polymers. N, N-dimethyl-α-(hydroxymethyl)acrylamide (DMαHAA) was (co)polymerized with N, N-diethylacrylamide (DEAA). Although the homopolymerization did not afford a polymeric product, the copolymerizations with various feed ratios yielded a series of the copolymers containing 0%–65% of DMαHAA units. The obtained copolymers exhibited a lower critical solution temperature (LCST) in water; the cloud points ( T cs) were linearly elevated as the contents of DMαHAA units from 32 to 64 °C, indicating that DMαHAA functioned as a more hydrophilic monomer than DEAA. The linear relationship between T c and DMαHAA content suggests that the homopolymer, poly(DMαHAA), should have T c at ca. 80 °C, although it is not available by direct radical homopolymerization.

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          Synthesis of Stimuli-Responsive Polymers by Living Polymerization: Poly(N-Isopropylacrylamide) and Poly(Vinyl Ether)s

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            Molecularly Imprinted Polymers with Stimuli-Responsive Affinity: Progress and Perspectives

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              Temperature responsive cellulose-graft-copolymers via cellulose functionalization in an ionic liquid and RAFT polymerization.

              Well-defined cellulose-graft-polyacrylamide copolymers were synthesized in a grafting-from approach by reversible addition-fragmentation chain transfer polymerization (RAFT). A chlorine moiety (degree of substitution DS(Cl) ≈ 1.0) was introduced into the cellulose using 1-butyl-3-methylimidazolium chloride (BMIMCl) as solvent before being substituted by a trithiocarbonate moiety resulting in cellulose macro-chain transfer agents (cellulose-CTA) with DS(RAFT) of 0.26 and 0.41. Poly(N,N-diethylacrylamide) (PDEAAm) and poly(N-isopropylacrylamide) (PNIPAM) were subsequently grafted from these cellulose-CTAs and the polymerization kinetics, the molecular weight characteristics and the product composition were studied by nuclear magnetic resonance spectroscopy, X-ray photoelectron spectroscopy, and size exclusion chromatography of the polyacrylamides after cleavage from the cellulose chains. The number-average molecular weights, Mn, of the cleaved polymers ranged from 1100 to 1600 g mol(-1) for PDEAAm (dispersity Đ = 1.4-1.8) and from 1200 to 2600 g mol (-1) for PNIPAM (Đ = 1.7-2.1). The LCST behavior of the cellulose-graft-copolymers was studied via the determination of cloud point temperatures, evidencing that the thermoresponsive properties of the hybrid materials could be finely tuned between 18 and 26 °C for PDEAAm and between 22 and 26 °C for PNIPAM side chains.
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                Author and article information

                Contributors
                Role: Academic Editor
                Journal
                Polymers (Basel)
                Polymers (Basel)
                polymers
                Polymers
                MDPI
                2073-4360
                20 October 2016
                October 2016
                : 8
                : 10
                : 374
                Affiliations
                Faculty of Textile Science and Technology, Shinshu University, Nagano 386-8567, Japan; 16fs515j@ 123456shinshu-u.ac.jp
                Author notes
                [* ]Correspondence: kohsaka@ 123456shinshu-u.ac.jp ; Tel.: +81-268-21-5488
                Article
                polymers-08-00374
                10.3390/polym8100374
                6431880
                5771082c-185e-4b04-85f9-75cb3b3f1815
                © 2016 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC-BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 12 September 2016
                : 14 October 2016
                Categories
                Article

                α-functionalized acrylamide,temperature-responsive polymer,lower critical solution temperature,hydrophilic monomer,radical polymerization

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